The pdhB gene encodes the beta subunit of the PDH complex, which is essential for cellular energy metabolism. In C. merolae, this enzyme operates under extreme environmental conditions (pH 1.5–2.5, temperatures up to 50°C), making it a model for studying thermostable metabolic machinery . The PDH complex in C. merolae likely supports mixotrophic growth, as the alga can utilize organic carbon sources like glycerol under heterotrophic conditions .
Recombinant pdhB is generated using genetic tools tailored for C. merolae’s chloroplast or nuclear genome:
Chloroplast Transformation: Stable integration of exogenous genes (e.g., cat for chloramphenicol resistance) is achieved via homologous recombination . Promoters such as psbD (light-inducible) and rbcL (cell cycle-dependent) drive high-efficiency expression .
Nuclear Transformation: Modular plasmids enable homologous recombination into the nuclear genome, with selection markers like chloramphenicol acetyltransferase (CAT) .
Metabolic Engineering: pdhB overexpression could enhance acetyl-CoA flux for lipid or terpenoid biosynthesis .
Extremophile Adaptations: Study of thermostable PDH complexes informs industrial enzyme design .
Organelle Division: Tools like heat-shock inducible systems (e.g., CMJ101C promoter) enable conditional pdhB expression to study mitochondrial-plastid coordination .
KEGG: cme:CymeCp128
STRING: 45157.CMV154CT